CA2063293A1 - Methods and compositions for inhibiting polymerization of vinyl monomers - Google Patents
Methods and compositions for inhibiting polymerization of vinyl monomersInfo
- Publication number
- CA2063293A1 CA2063293A1 CA002063293A CA2063293A CA2063293A1 CA 2063293 A1 CA2063293 A1 CA 2063293A1 CA 002063293 A CA002063293 A CA 002063293A CA 2063293 A CA2063293 A CA 2063293A CA 2063293 A1 CA2063293 A1 CA 2063293A1
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- Prior art keywords
- compound
- composition
- organic amine
- dihydroxybenzene
- fouling
- Prior art date
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-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1826—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms poly-hydroxy
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
ABSTRACT
Methods and compositions are provided for inhibiting the polymerization of a vinyl monomer during elevated processing thereof or during storage or shipment of the monomer containing product. The compositions comprise a combination of a dihydroxybenzene compound and an organic amine compound.
Methods and compositions are provided for inhibiting the polymerization of a vinyl monomer during elevated processing thereof or during storage or shipment of the monomer containing product. The compositions comprise a combination of a dihydroxybenzene compound and an organic amine compound.
Description
METHODS AND COMPOSITIONS FOR INHIBITING
POLYMERIZATION OF VINYL MONOMERS
FIELD OF THE INVENTION
This invention relates to methods and compositions for inhibiting the undesired polymerization of vinyl monomers and subsequent fouling of heat exchangers in refinery and petrochemical processing systems.
BACKGROUND OF THE INVENTION
Fouling can be defined as the accumulation of unwanted matter on heat transfer surfaces. This deposition can be very costly in refinery and petrochemical plants since it increases fuel usage, results in interrupted operations and production losses and increases maintenance costs.
Deposits are found in a variety of equipment: preheat exchangers, overhead condensers, furnaces, heat exchangers, fractionating towers, reboilers, compressors and reactor beds.
~ ,3 These deposits are complex but they can be broadly characterized as organic and inorganic. They consist of metal oxides and sulfides, soluble organic metals, organic polymers, coke, salt and various other particulate matter.
The chemical composition of organic foulants is rarely identified completely. Organic fouling is caused by insoluble polymers which sometimes are degraded to coke. The polymers are usually formed by reactions of unsaturated hydrocarbons, although any hydrocarbon can polymerize. Generally, olefins tend to polymerize more readily than aromatics, which in turn polymerize more readily than paraffins. Trace organic materials containing Hetero atoms such as nitrogen, oxygen and sulfur also contribute to polymerization.
Polymers are generally formed by free radical chain reactions. These reactions, shown below, consist of two phases, an initiation phase and a propagation phase. In Reaction 1, the chain initiation reaction, a free radical represented by R-, is formed (the symbol R- can be any hydrocarbon). These free radicals, which have an odd electron, act as chain carriers. During chain propagation, additional free radicals are Formed and the hydrocarbon molecules (R) grow larger and larger (see Reaction 4), forming the unwanted polymers which accumulate on heat transfer surfaces.
Chain reactions can be triggered in several ways. In Reaction 1, heat starts the chain. Example: When a reactive molecule such as an olefin or a diolefin is heated, a free radical is produced. Another way a chain reaction starts is shown in Reaction 3. Metal ions initiate free radical formation here.
Accelerating polymerization by oxygen and metals can be seen by reviewing Reactions 2 and 3.
As polymers form, more polymers begin to adhere to the heat transfer surfaces. This adherence results in dehydrogenation of the hydrocarbon and eventually the polymer is converted to coke.
1. Chain Initiation R - H --- R- + H-
POLYMERIZATION OF VINYL MONOMERS
FIELD OF THE INVENTION
This invention relates to methods and compositions for inhibiting the undesired polymerization of vinyl monomers and subsequent fouling of heat exchangers in refinery and petrochemical processing systems.
BACKGROUND OF THE INVENTION
Fouling can be defined as the accumulation of unwanted matter on heat transfer surfaces. This deposition can be very costly in refinery and petrochemical plants since it increases fuel usage, results in interrupted operations and production losses and increases maintenance costs.
Deposits are found in a variety of equipment: preheat exchangers, overhead condensers, furnaces, heat exchangers, fractionating towers, reboilers, compressors and reactor beds.
~ ,3 These deposits are complex but they can be broadly characterized as organic and inorganic. They consist of metal oxides and sulfides, soluble organic metals, organic polymers, coke, salt and various other particulate matter.
The chemical composition of organic foulants is rarely identified completely. Organic fouling is caused by insoluble polymers which sometimes are degraded to coke. The polymers are usually formed by reactions of unsaturated hydrocarbons, although any hydrocarbon can polymerize. Generally, olefins tend to polymerize more readily than aromatics, which in turn polymerize more readily than paraffins. Trace organic materials containing Hetero atoms such as nitrogen, oxygen and sulfur also contribute to polymerization.
Polymers are generally formed by free radical chain reactions. These reactions, shown below, consist of two phases, an initiation phase and a propagation phase. In Reaction 1, the chain initiation reaction, a free radical represented by R-, is formed (the symbol R- can be any hydrocarbon). These free radicals, which have an odd electron, act as chain carriers. During chain propagation, additional free radicals are Formed and the hydrocarbon molecules (R) grow larger and larger (see Reaction 4), forming the unwanted polymers which accumulate on heat transfer surfaces.
Chain reactions can be triggered in several ways. In Reaction 1, heat starts the chain. Example: When a reactive molecule such as an olefin or a diolefin is heated, a free radical is produced. Another way a chain reaction starts is shown in Reaction 3. Metal ions initiate free radical formation here.
Accelerating polymerization by oxygen and metals can be seen by reviewing Reactions 2 and 3.
As polymers form, more polymers begin to adhere to the heat transfer surfaces. This adherence results in dehydrogenation of the hydrocarbon and eventually the polymer is converted to coke.
1. Chain Initiation R - H --- R- + H-
2. Chain Propagation a. R- + 2 --~ R-O-O
b. R - O - O + R' - H ~ R- + R-O-O-H
c. R'- + C = C --~ R'-C - C --~ Polymer
b. R - O - O + R' - H ~ R- + R-O-O-H
c. R'- + C = C --~ R'-C - C --~ Polymer
3. Chain Initiation a. Me++ + RH --~ Me+ R- + H+
b. Me++ + R-O-O-H -~ Me+ R-O-O ~ H+
b. Me++ + R-O-O-H -~ Me+ R-O-O ~ H+
4. Chain Termination a. R- + R- --~ R - R' b. R- + R-O-O -~ R-O-O-R
In refineries, deposits usually contain both organic and inorganic compounds. This makes the identification of the exact cause of fouling extremely difficult. Even if it were possible to precisely identify every single deposit constituent, this would not guarantee uncovering the cause of the problem. Assumptions are often erroneously made that if a deposit is predominantly a certain compound, then that compound is the cause of the fouling. In reality, oftentimes a minor constituent in the deposit could be acting as a binder, a catalyst, or in some other role that influences actual deposit formation.
The final form of the deposit as viewed by analytical chemists may not always indicate its origin or cause. Before openings, equipment is steamed, water-washed, or otherwise readied for inspection. During this preparation, fouling matter can be changed both physically and chemically. For example, water-soluble salts can be washed away or certain deposit constituents oxidized to another form.
In petrochemical plants, fouling matter is often organic in nature. Fouling can be severe when monomers convert to polymers before they leave the plant. This is most likely to happen in streams high in ethylene, propylene, butadiene, styrene and other unsaturates. Probable locations for such reactions include units where the unsaturates are being handled or purified, or in streams which contain these reactive materials only as contaminants.
Zg~ ?~33 Even through some petrochemical fouling problems seem similar, subtle differences in feedstock, processing schemes, processing equipment and type of contaminants can lead to variations in fouling severity. For example, ethylene plant depropanizer reboilers experience fouling that appears to be primarily polybutadiene in nature. The severity of the problem varies significantly from plant to plant, however. The average reboiler run length may vary from one to two weeks up to four to six months (without chemical treatment).
Although it is usually impractical to identify the fouling problem by analytical techniques alone, this information combined with knowledge of the process, processing conditions and the factors known to contribute to fouling, are all essential to understanding the problem.
There are many ways to reduce fouling both mechanically and chemically. Chemical additives often offer an effective anti-fouling means; however, processing changes, mechanical modifications equipment and other methods available to the plant should not be overlooked.
Antifoulant chemicals are formulated from several materials: some prevent foulants from forming, others prevent foulants from depositing on heat transfer equipment. Materials that prevent deposit formation include antioxidants, metal coordinators and corrosion inhibitors. Compounds that prevent deposition are surfactants which act as detergents or dispersants.
,: . :, : , - :- .
:
,, , , , , , , . - . , .:
. , ~ , ~?~ s~3 Different combinations of these properties are blended together to maximize results for each different application. These "poly-functional" antifoulants are generally more versatile and effective since they can be designed to combat various types of fouling that can be present in any given system.
Research indicates that even very small amounts of oxygen can cause or accelerate polymerization. Accordingly, anti-oxidant-type antifoulants have been developed to prevent oxygen from initiating polymerization. Antioxidants act as chain-stoppers by forming inert molecules with the oxidized free radical hydrocarbons, in accordance with the following reaction:
Chain Termination ROO Antioxidant ~ ROOH + Antioxidant (H) Surface modifiers or detergents change metal surface charac teristics to prevent foulants from depositing. Dispersants or stabilizers prevent insoluble polymers, coke and other particulate matter from agglomerating into large particles which can settle out of the process stream and adhere to the metal surfaces of process equipment. They also modify the particle surface so that polymeri-zation cannot readily take place.
Antifoulants are designed to prevent equipment surfacesFrom fouling. They are not designed to clean up existing foulants.
Therefore, an antifoulant should be started immediately after equip-ment is cleaned. It is usually advantageous to pretreat the system 2~.~?93 at double the recommended dosage for two or three weeks to reduce the initial high rate of fouling immediately after startup.
The increased profit possible with the use of antifoulants varies from application to application. It can include an increase in production, fuel savings, maintenance savings and other savings from greater operating efficiency.
There are many areas in the hydrocarbon processing industry where antifoulants have been used extensively; the main areas of treatment are discussed below.
In a refinery, the crude unit has been the focus of atten-tion because of increased fuel costs. Antifoulants have been successfully applied at the exchangers; downstream and upstream of the desalter, on the product side of the preheat train, on both sides of the desalter makeup water exchanger and at the sour water stripper.
Hydrodesulfurization units of all types experience preheat fouling problems. Among those that have been successfully treated are reformer pretreaters processing both straight run and coker naphtha, desulfurizers processing catalytically cracked and coker gas oil, and distillate hydro-treaters. In one case, fouling of a Unifiner stripper column was solved by applying a corrosion inhibitor upstream of the problem source.
.
- .
. . .
: .. ' ~-.. -. ~
s~ ~7~3 Unsaturated and saturated gas plants (refinery vapor recovery units) experience fouling in the various -fractionation columns, reboilers and compressors. In some cases, a corrosion control program combined with an antifoulant program gave the best results. In other cases, an application of antifoulants alone was enough to solve the problem.
Cat cracker preheat exchanger fouling, both at the vacuum column and at the cat cracker itse'lf, has also been corrected by the use of antifoulants.
The two most preva'lent areas for fouling problems in petro-chemical plants are at the ethylene and styrene plants. In an ethylene plant, the furnace gas compressors, the various fraction-ating columns and reboilers are subject to fouling. Polyfunctional antifoulants, for the most part, have provided good results in these areas. Fouling can also be a problem at the butadiene extraction area. Both antioxidants and polyfunctional antifoulants have been used with good results.
In the different design butadiene plants, absorption oil fouling and distillation column and reboiler fouling have been corrected with various types of antifoulants.
Chlorinated hydrocarbon plants, such as VCM, EDC and perchloroethane and tri-ch'loroethane have all experienced various types of fouling problems. The metal coordinating/antioxidant-type antifoulants give excellent service in these areas.
2~ 3 SUMMARY OF THE INVENTION
The present invention provides for polymerization inhibiting compositions comprising an organic amine compound and a dihydroxybenzene compound.
The present invention further provides for methods for inhibiting the polymerization of vinyl monomers during the processing of hydrocarbons. The use of an organic amine and a dihydroxybenzene compound will inhibit the formation of polymers and will inhibit the fouling of heat transfer surfaces in contact with the hydrocarbon being processed.
DESCRIPTION OF THE RELATED ART
U.S. Patent 4,744,881 (Reid) teaches the use of a composition of an unhindered or hindered phenol and a strongly basic amine compound to control fouling in hydrocarbon fluids having a bromine number greater than 10. This patent discloses N-(2-aminoethyl) piperazine as one of the amines that can be utilized in the process.
U.S. Patent 2,329,251, (Chenicek) teaches an early method of inhibiting gum formation in hydrocarbon distillates using an alkylene polyamine salt of an organic acid.
U.S. Patent 4,647,290 (Reid) teaches the use of a compo-sition of N-(2-aminoethyl) piperazine and N,N-diethylhydroxylamine to inhibit color deterioration of distillate fuel oils. The combination of these two chemicals provide a more e~Fective color stabilized composition than when either is used alone.
U.S. Patent No. 4,867,754 (Reid) teaches the use of a composition of a phosphite compound and an organic compound containing a tertiary amine of the formula T3N to stabilize distillate fuel oils. 2-(aminoethyl) pipera7ine is disclosed as one of the possible amines used. This combination provides a higher degree of stabilization of distillate fuel oil than when the individual species are used alone.
U.S. Patent No. 4,011,057 (Sayers) discloses an antioxidant composition especially for gasoline. The composition comprises a hindered phenol and an amino compound having a PKb of from about 0.3 to 8Ø
U.S. Patent No. 4,456,526 (Miller et al.) discloses an antifoulant composition and method for inhibiting fouling in petroleum processing equipment. The composition comprises 10 to ~0 90 weight percent of an N,N-dialkylhydroxylamine compound having alkyl groups from 2 to 10 carbon atoms and 90 to 10 weight percent of a tertiary-alkyl catechol having 4 to 20 alkyl carbon atoms in an inert solvent.
U.S. Patent No. 4,929,778 (Roling) discloses a composition and method for inhibiting polymerization of styrene monomer during its processing or shipment. The composition which can inhibit fouling of processing equipment comprises a pnenylenediamine compound and a hindered phenol compound.
U.S. Patent No. 4~810,354 (Roling et al.) discloses a method of inhibiting fouling in a hydrocarbon by deactivating transition metal impurities in the hydrocarbon. This method employs adding an alkoxylated Mannich product formed by reacting an alkoxylated phenol, a polyamine and an aldehyde.
U.S. Patent No. 4,8~4,45~ (Forester) discloses an antifouling treatment for petroleum hydrocarbons. The treatment comprises adding to the hydrocarbon an amine salt of polyalkenylthiophosphonic acid. The amines of the present invention could be used to react with the acid to form the amine salt.
DETAILED DESCRIPTION OF THE INVENTION
The pres'ent in~ention pertains to methods and compositions for inhibiting the polymerization of vinyl monomers during the processing of hydrocarbons. The polymerization inhibiting composition is a combination of an organic amine and a dihydroxybenzene compound.
2~ 3 The phrase "vinyl monomers" as herein used is intended to include compounds having the vinyl grouping including, for instance, styrene, methyl methacrylate, and acrylonitrile.
The dihydroxybenzene compounds have the formula o~ o~
s ~ ~o~$
wherein R is H, alkyl or aryl. -Exemplary dihydroxybenzene compounds include, but are not limited to, hydroquinone, tert-butyl hydroquinone, tert-butyl catechol and resorcinol.
The organic amines generally have the formula NR2R3R4 where R2, R3 and R4 are hydrogen, alkyl, aryl, or substituted alkyl or aryl or in any combination thereof. Exemplary amines include polyoxypropylenediamine, diethylenetriamine, ethylenediamine and triethylenetetramine.
The treatment range for the composition, i.e., amine/di-hydroxybenzene, clearly depends upon the severity of the fouling problem due to free radical polymerization encountered as well as the activity and constituency of the combination utilized.
For this reason, the success of the treatment is totally dependent upon the use of a sufficient amount of the purpose of whatever the i ,. . . ~ ... ;.;
; . : . . : . .~.
:~
. . . .
, ~ ~ ~r~
composition of choice is. Broadly speaking, the treatment recom-mended could be in a range from about l part per million to about 5000 parts per million of the hydrocarbon being processed. Prefer-ably a range from about 5 parts per million to about 100 parts per million of hydrocarbon is employed.
The amount by weight (active) of the amine to the dihydroxy-benzen~ ranges from 0.001% to 0.5% and preferably is 0.0025% to 0.005% of the total treatment.
The weight ratio of the components is 60 to 40% amine com-pound to 40 to 60% dihydroxybenzene compound. Preferably, the weight ratio is 60% amine compound and 40% dihydroxybenzene compound. A preferred embodiment employs 60% by weight diethylene-triamine and 40% hydroquinone.
The method of the present invention can control the fouling of processing equipment, such as the equipment used in separation and purification processes by vinyl monomers, which is due to or caused by the polymerization of the monomer. The instant invention may be used as both a process inhibitor, which is employed during preparation and processiny (e.g., employing heat) of the vinyl mono-mer, and as a product inhibitor, which is combined with the monomerin order to inhibit polymerization during storage and handling.
The dihydroxybenzene compound and organic amine can be added to the vinyl monomer by any conventional method. The components can be added to the monomer as a single composition ~?d~ 3 containing the inhibitor compounds or the individual components can be added separately or in any other desired combination.
The composition may be added as either a dispersion or as a solution using a suitable liquid carrier dispersing medium or solvent which is compatible with the monomer. Preferably, a solution is provided and the solvent is a non-polar organic solvent such as xylene (a commercial mixture of o, m and p isomers), or heavy aromatic naphtha.
The data set forth below were developed to demonstrate the unexpected results occasioned by use of the invention. The following examples are included as being illustrations of the invention and should not be construed as limiting the scope thereof.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Vapor Phase Apparatus Test The vapor phase apparatus consists of a syringe pump that injects the monomer at a fixed rate into a vaporization tube.
The vaporization tube is 1~ inches long and has a one-quarter of an inch inside d;ameter. This stainless steel tube is heated to 350 to 450F (at least 70F above the boiling point of the monomer).
e ~ 9,~, 20 ml oh monomer is inJected uniformly over a period of 15 minutes into this 11 ml capacity tube (a residence time of 8 minutes was calculated) in which time the liquid reached vapori-zation temperatures.
A 4 inch long by one-quarter inch inside diameter steel tube containing 0.5 9 of steel wool, called a demister, is placed at the end of the vaporization tube to prevent any liquid droplets from entraining into the deposition tube. The deposition tube consists of a 12 inch long by one-quarter inch inside diameter stainless steel tube containing 4.5 9 of packed steel wool. The deposition tube is weighed before and after each test to measure the amount of polymer formed.
The vapori~ation tube and deposition tube are wrapped separately with heating tapes which were controlled at specific voltages. Thermocouples wrapped in the heating tapes were used to record the temperatures on the outslde tube surfaces. Results are reported in Table 1.
TAB~E I
Treatment (lOOO Ppm) DePosit (mg) ~ 248.0 A 217.0 B 299.0 B 415.0 C 1200.0 C 793.0 C 994.0 TABLE I (Cont'd) Treatment ~lOOC pPm)Deposit ~mq) D 2~6.0 E 8.2 E 3.2 F 411.0 F 809.0 F 849.0 B/F 2.1 B/F 6.9 B/F 5.7 G 356.0 G 588.0 G 538.0 Blank 1300.0 Blank 1600.0 Blank 1300.0 Blank 1100.0 A = Amine succinimide dispersant B = Polyoxypropylenediamine C = DEHA = diethylhydroxylamine D = Diethylenetriamine E = DNOC = 4, 6-dinitrocreosol F = Hydroquinone G = Triethylenetetramine It can be seen from Table I that the dihydroxybenzerle/
amine combination (i.e., B/F), specifically hydroquinone and poly-oxypropylenediamine, proved more efficacious as an antifoulant composition than those used in the art.
Due to the unexpected results shown by the combination of dihydroxybenzene compound and organic amine, it is possible to produce a more effective monomer polymerization inhibiting ~r~ 3 treatment than is obtainable by either ingredient alone when measured at comparable treatment levels. This enhanced inhibition activity of the mix-ture allows the concentration of each ingredient to be lowered and the total quantity of the polymerization inhibitor required for an effective treatment at elevated temperatures may be reduced. This factor is especially important in monomer purification procedures where the obvious goal of the process is to provide high level monomer purity.
The term "elevated temperatures" as used herein means temperatures of from about 100 to 300F that are commonly encountered during the heat treatment of vinyl monomers. Such heat treatment procedures include distillation and various other processes.
While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications will be obvious to those skilled in the art. The appended claims should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.
In refineries, deposits usually contain both organic and inorganic compounds. This makes the identification of the exact cause of fouling extremely difficult. Even if it were possible to precisely identify every single deposit constituent, this would not guarantee uncovering the cause of the problem. Assumptions are often erroneously made that if a deposit is predominantly a certain compound, then that compound is the cause of the fouling. In reality, oftentimes a minor constituent in the deposit could be acting as a binder, a catalyst, or in some other role that influences actual deposit formation.
The final form of the deposit as viewed by analytical chemists may not always indicate its origin or cause. Before openings, equipment is steamed, water-washed, or otherwise readied for inspection. During this preparation, fouling matter can be changed both physically and chemically. For example, water-soluble salts can be washed away or certain deposit constituents oxidized to another form.
In petrochemical plants, fouling matter is often organic in nature. Fouling can be severe when monomers convert to polymers before they leave the plant. This is most likely to happen in streams high in ethylene, propylene, butadiene, styrene and other unsaturates. Probable locations for such reactions include units where the unsaturates are being handled or purified, or in streams which contain these reactive materials only as contaminants.
Zg~ ?~33 Even through some petrochemical fouling problems seem similar, subtle differences in feedstock, processing schemes, processing equipment and type of contaminants can lead to variations in fouling severity. For example, ethylene plant depropanizer reboilers experience fouling that appears to be primarily polybutadiene in nature. The severity of the problem varies significantly from plant to plant, however. The average reboiler run length may vary from one to two weeks up to four to six months (without chemical treatment).
Although it is usually impractical to identify the fouling problem by analytical techniques alone, this information combined with knowledge of the process, processing conditions and the factors known to contribute to fouling, are all essential to understanding the problem.
There are many ways to reduce fouling both mechanically and chemically. Chemical additives often offer an effective anti-fouling means; however, processing changes, mechanical modifications equipment and other methods available to the plant should not be overlooked.
Antifoulant chemicals are formulated from several materials: some prevent foulants from forming, others prevent foulants from depositing on heat transfer equipment. Materials that prevent deposit formation include antioxidants, metal coordinators and corrosion inhibitors. Compounds that prevent deposition are surfactants which act as detergents or dispersants.
,: . :, : , - :- .
:
,, , , , , , , . - . , .:
. , ~ , ~?~ s~3 Different combinations of these properties are blended together to maximize results for each different application. These "poly-functional" antifoulants are generally more versatile and effective since they can be designed to combat various types of fouling that can be present in any given system.
Research indicates that even very small amounts of oxygen can cause or accelerate polymerization. Accordingly, anti-oxidant-type antifoulants have been developed to prevent oxygen from initiating polymerization. Antioxidants act as chain-stoppers by forming inert molecules with the oxidized free radical hydrocarbons, in accordance with the following reaction:
Chain Termination ROO Antioxidant ~ ROOH + Antioxidant (H) Surface modifiers or detergents change metal surface charac teristics to prevent foulants from depositing. Dispersants or stabilizers prevent insoluble polymers, coke and other particulate matter from agglomerating into large particles which can settle out of the process stream and adhere to the metal surfaces of process equipment. They also modify the particle surface so that polymeri-zation cannot readily take place.
Antifoulants are designed to prevent equipment surfacesFrom fouling. They are not designed to clean up existing foulants.
Therefore, an antifoulant should be started immediately after equip-ment is cleaned. It is usually advantageous to pretreat the system 2~.~?93 at double the recommended dosage for two or three weeks to reduce the initial high rate of fouling immediately after startup.
The increased profit possible with the use of antifoulants varies from application to application. It can include an increase in production, fuel savings, maintenance savings and other savings from greater operating efficiency.
There are many areas in the hydrocarbon processing industry where antifoulants have been used extensively; the main areas of treatment are discussed below.
In a refinery, the crude unit has been the focus of atten-tion because of increased fuel costs. Antifoulants have been successfully applied at the exchangers; downstream and upstream of the desalter, on the product side of the preheat train, on both sides of the desalter makeup water exchanger and at the sour water stripper.
Hydrodesulfurization units of all types experience preheat fouling problems. Among those that have been successfully treated are reformer pretreaters processing both straight run and coker naphtha, desulfurizers processing catalytically cracked and coker gas oil, and distillate hydro-treaters. In one case, fouling of a Unifiner stripper column was solved by applying a corrosion inhibitor upstream of the problem source.
.
- .
. . .
: .. ' ~-.. -. ~
s~ ~7~3 Unsaturated and saturated gas plants (refinery vapor recovery units) experience fouling in the various -fractionation columns, reboilers and compressors. In some cases, a corrosion control program combined with an antifoulant program gave the best results. In other cases, an application of antifoulants alone was enough to solve the problem.
Cat cracker preheat exchanger fouling, both at the vacuum column and at the cat cracker itse'lf, has also been corrected by the use of antifoulants.
The two most preva'lent areas for fouling problems in petro-chemical plants are at the ethylene and styrene plants. In an ethylene plant, the furnace gas compressors, the various fraction-ating columns and reboilers are subject to fouling. Polyfunctional antifoulants, for the most part, have provided good results in these areas. Fouling can also be a problem at the butadiene extraction area. Both antioxidants and polyfunctional antifoulants have been used with good results.
In the different design butadiene plants, absorption oil fouling and distillation column and reboiler fouling have been corrected with various types of antifoulants.
Chlorinated hydrocarbon plants, such as VCM, EDC and perchloroethane and tri-ch'loroethane have all experienced various types of fouling problems. The metal coordinating/antioxidant-type antifoulants give excellent service in these areas.
2~ 3 SUMMARY OF THE INVENTION
The present invention provides for polymerization inhibiting compositions comprising an organic amine compound and a dihydroxybenzene compound.
The present invention further provides for methods for inhibiting the polymerization of vinyl monomers during the processing of hydrocarbons. The use of an organic amine and a dihydroxybenzene compound will inhibit the formation of polymers and will inhibit the fouling of heat transfer surfaces in contact with the hydrocarbon being processed.
DESCRIPTION OF THE RELATED ART
U.S. Patent 4,744,881 (Reid) teaches the use of a composition of an unhindered or hindered phenol and a strongly basic amine compound to control fouling in hydrocarbon fluids having a bromine number greater than 10. This patent discloses N-(2-aminoethyl) piperazine as one of the amines that can be utilized in the process.
U.S. Patent 2,329,251, (Chenicek) teaches an early method of inhibiting gum formation in hydrocarbon distillates using an alkylene polyamine salt of an organic acid.
U.S. Patent 4,647,290 (Reid) teaches the use of a compo-sition of N-(2-aminoethyl) piperazine and N,N-diethylhydroxylamine to inhibit color deterioration of distillate fuel oils. The combination of these two chemicals provide a more e~Fective color stabilized composition than when either is used alone.
U.S. Patent No. 4,867,754 (Reid) teaches the use of a composition of a phosphite compound and an organic compound containing a tertiary amine of the formula T3N to stabilize distillate fuel oils. 2-(aminoethyl) pipera7ine is disclosed as one of the possible amines used. This combination provides a higher degree of stabilization of distillate fuel oil than when the individual species are used alone.
U.S. Patent No. 4,011,057 (Sayers) discloses an antioxidant composition especially for gasoline. The composition comprises a hindered phenol and an amino compound having a PKb of from about 0.3 to 8Ø
U.S. Patent No. 4,456,526 (Miller et al.) discloses an antifoulant composition and method for inhibiting fouling in petroleum processing equipment. The composition comprises 10 to ~0 90 weight percent of an N,N-dialkylhydroxylamine compound having alkyl groups from 2 to 10 carbon atoms and 90 to 10 weight percent of a tertiary-alkyl catechol having 4 to 20 alkyl carbon atoms in an inert solvent.
U.S. Patent No. 4,929,778 (Roling) discloses a composition and method for inhibiting polymerization of styrene monomer during its processing or shipment. The composition which can inhibit fouling of processing equipment comprises a pnenylenediamine compound and a hindered phenol compound.
U.S. Patent No. 4~810,354 (Roling et al.) discloses a method of inhibiting fouling in a hydrocarbon by deactivating transition metal impurities in the hydrocarbon. This method employs adding an alkoxylated Mannich product formed by reacting an alkoxylated phenol, a polyamine and an aldehyde.
U.S. Patent No. 4,8~4,45~ (Forester) discloses an antifouling treatment for petroleum hydrocarbons. The treatment comprises adding to the hydrocarbon an amine salt of polyalkenylthiophosphonic acid. The amines of the present invention could be used to react with the acid to form the amine salt.
DETAILED DESCRIPTION OF THE INVENTION
The pres'ent in~ention pertains to methods and compositions for inhibiting the polymerization of vinyl monomers during the processing of hydrocarbons. The polymerization inhibiting composition is a combination of an organic amine and a dihydroxybenzene compound.
2~ 3 The phrase "vinyl monomers" as herein used is intended to include compounds having the vinyl grouping including, for instance, styrene, methyl methacrylate, and acrylonitrile.
The dihydroxybenzene compounds have the formula o~ o~
s ~ ~o~$
wherein R is H, alkyl or aryl. -Exemplary dihydroxybenzene compounds include, but are not limited to, hydroquinone, tert-butyl hydroquinone, tert-butyl catechol and resorcinol.
The organic amines generally have the formula NR2R3R4 where R2, R3 and R4 are hydrogen, alkyl, aryl, or substituted alkyl or aryl or in any combination thereof. Exemplary amines include polyoxypropylenediamine, diethylenetriamine, ethylenediamine and triethylenetetramine.
The treatment range for the composition, i.e., amine/di-hydroxybenzene, clearly depends upon the severity of the fouling problem due to free radical polymerization encountered as well as the activity and constituency of the combination utilized.
For this reason, the success of the treatment is totally dependent upon the use of a sufficient amount of the purpose of whatever the i ,. . . ~ ... ;.;
; . : . . : . .~.
:~
. . . .
, ~ ~ ~r~
composition of choice is. Broadly speaking, the treatment recom-mended could be in a range from about l part per million to about 5000 parts per million of the hydrocarbon being processed. Prefer-ably a range from about 5 parts per million to about 100 parts per million of hydrocarbon is employed.
The amount by weight (active) of the amine to the dihydroxy-benzen~ ranges from 0.001% to 0.5% and preferably is 0.0025% to 0.005% of the total treatment.
The weight ratio of the components is 60 to 40% amine com-pound to 40 to 60% dihydroxybenzene compound. Preferably, the weight ratio is 60% amine compound and 40% dihydroxybenzene compound. A preferred embodiment employs 60% by weight diethylene-triamine and 40% hydroquinone.
The method of the present invention can control the fouling of processing equipment, such as the equipment used in separation and purification processes by vinyl monomers, which is due to or caused by the polymerization of the monomer. The instant invention may be used as both a process inhibitor, which is employed during preparation and processiny (e.g., employing heat) of the vinyl mono-mer, and as a product inhibitor, which is combined with the monomerin order to inhibit polymerization during storage and handling.
The dihydroxybenzene compound and organic amine can be added to the vinyl monomer by any conventional method. The components can be added to the monomer as a single composition ~?d~ 3 containing the inhibitor compounds or the individual components can be added separately or in any other desired combination.
The composition may be added as either a dispersion or as a solution using a suitable liquid carrier dispersing medium or solvent which is compatible with the monomer. Preferably, a solution is provided and the solvent is a non-polar organic solvent such as xylene (a commercial mixture of o, m and p isomers), or heavy aromatic naphtha.
The data set forth below were developed to demonstrate the unexpected results occasioned by use of the invention. The following examples are included as being illustrations of the invention and should not be construed as limiting the scope thereof.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Vapor Phase Apparatus Test The vapor phase apparatus consists of a syringe pump that injects the monomer at a fixed rate into a vaporization tube.
The vaporization tube is 1~ inches long and has a one-quarter of an inch inside d;ameter. This stainless steel tube is heated to 350 to 450F (at least 70F above the boiling point of the monomer).
e ~ 9,~, 20 ml oh monomer is inJected uniformly over a period of 15 minutes into this 11 ml capacity tube (a residence time of 8 minutes was calculated) in which time the liquid reached vapori-zation temperatures.
A 4 inch long by one-quarter inch inside diameter steel tube containing 0.5 9 of steel wool, called a demister, is placed at the end of the vaporization tube to prevent any liquid droplets from entraining into the deposition tube. The deposition tube consists of a 12 inch long by one-quarter inch inside diameter stainless steel tube containing 4.5 9 of packed steel wool. The deposition tube is weighed before and after each test to measure the amount of polymer formed.
The vapori~ation tube and deposition tube are wrapped separately with heating tapes which were controlled at specific voltages. Thermocouples wrapped in the heating tapes were used to record the temperatures on the outslde tube surfaces. Results are reported in Table 1.
TAB~E I
Treatment (lOOO Ppm) DePosit (mg) ~ 248.0 A 217.0 B 299.0 B 415.0 C 1200.0 C 793.0 C 994.0 TABLE I (Cont'd) Treatment ~lOOC pPm)Deposit ~mq) D 2~6.0 E 8.2 E 3.2 F 411.0 F 809.0 F 849.0 B/F 2.1 B/F 6.9 B/F 5.7 G 356.0 G 588.0 G 538.0 Blank 1300.0 Blank 1600.0 Blank 1300.0 Blank 1100.0 A = Amine succinimide dispersant B = Polyoxypropylenediamine C = DEHA = diethylhydroxylamine D = Diethylenetriamine E = DNOC = 4, 6-dinitrocreosol F = Hydroquinone G = Triethylenetetramine It can be seen from Table I that the dihydroxybenzerle/
amine combination (i.e., B/F), specifically hydroquinone and poly-oxypropylenediamine, proved more efficacious as an antifoulant composition than those used in the art.
Due to the unexpected results shown by the combination of dihydroxybenzene compound and organic amine, it is possible to produce a more effective monomer polymerization inhibiting ~r~ 3 treatment than is obtainable by either ingredient alone when measured at comparable treatment levels. This enhanced inhibition activity of the mix-ture allows the concentration of each ingredient to be lowered and the total quantity of the polymerization inhibitor required for an effective treatment at elevated temperatures may be reduced. This factor is especially important in monomer purification procedures where the obvious goal of the process is to provide high level monomer purity.
The term "elevated temperatures" as used herein means temperatures of from about 100 to 300F that are commonly encountered during the heat treatment of vinyl monomers. Such heat treatment procedures include distillation and various other processes.
While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications will be obvious to those skilled in the art. The appended claims should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.
Claims (19)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A vinyl monomer polymerization inhibiting composition comprising a dihydroxybenzene compound and an organic amine compound.
2. The composition as claimed in claim 1 wherein said dihydroxybenzene compound has the formula wherein the OH groups can be meta, ortho or para to each other and R is a hydrogen, alkyl or aryl group.
3. The composition as claimed in claim 2 wherein said dihydroxybenzene compound is hydroquinone.
4. The composition as claimed in claim 1 wherein said organic amine group has the formula wherein R2, R3 and R4 are hydrogen, alkyl, aryl, or substituted alkyl or aryl group.
5. The composition as claimed in claim 4 wherein said organic amine compound is polyoxypropylenediamine.
6. The composition as claimed in claim 4 wherein said organic amine compound is diethylenetriamine.
7. The composition as claimed in claim 1 wherein said dihydroxybenzene and said organic amine compound are dissolved in a non-polar organic solvent.
~ . The composition as claimed in claim 7 wherein said solvent is xylene.
9. The composition as claimed in claim 1 wherein the weight ratio of said dihydroxybenzene compound to said organic amine compound is 40 to 60%:60 to 40%.
10. A method for inhibiting the polymerization of vinyl monomer compounds comprising adding to said vinyl monomer compound an effective inhibiting amount of (a) a dihydroxybenzene compound and (b) an organic amine compound.
11. The method as claimed in claim 10 wherein said dihydroxybenzene compound has the formula wherein the OH groups can be meta, para or ortho to each other and R is a hydrogen, alkyl or aryl group.
12. The method as claimed in claim 11 wherein said dihydroxybenzene compound is hydroquinone.
13. The method as claimed in claim 10 wherein said organic amine compound has the formula wherein R2, R3 and R4 are hydrogen, alkyl, aryl, or substituted alkyl or aryl group.
14. The method as claimed in claim 13 wherein said organic amine compound is polyoxypropylenediamine.
15. The method as claimed in claim 13 wherein said organic amine compound is diethylenetriamine.
16. The method as claimed in claim 10 comprising adding to said vinyl monomer compound from about 1 to about 5000 parts of said polymerization inhibitor per million parts of said vinyl monomer compound.
17. The method as claimed in claim 16 comprising adding to said vinyl monomer compound from about 5 to about 100 parts of said polymerization inhibitor per million parts of said vinyl monomer compound.
18. The method as claimed in claim 10 wherein said dihydroxybenzene compound and said organic amine compound are dissolved in a non-polar organic solvent.
19. The method as claimed in claim 18 wherein said solvent is xylene.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/733,480 US5221498A (en) | 1991-07-22 | 1991-07-22 | Methods and compositions for inhibitoring polymerization of vinyl monomers |
| US07/733,480 | 1991-07-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2063293A1 true CA2063293A1 (en) | 1993-01-23 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002063293A Abandoned CA2063293A1 (en) | 1991-07-22 | 1992-03-18 | Methods and compositions for inhibiting polymerization of vinyl monomers |
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| Country | Link |
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| US (1) | US5221498A (en) |
| CA (1) | CA2063293A1 (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5756870A (en) * | 1996-05-03 | 1998-05-26 | Betzdearborn Inc. | Methods for inhibiting the polymerization of ethylenically unsaturated monomers |
| US6200461B1 (en) * | 1998-11-05 | 2001-03-13 | Betzdearborn Inc. | Method for inhibiting polymerization of ethylenically unsaturated hydrocarbons |
| US6673232B2 (en) * | 2000-07-28 | 2004-01-06 | Atofina Chemicals, Inc. | Compositions for mitigating coke formation in thermal cracking furnaces |
| US6579442B2 (en) * | 2001-05-22 | 2003-06-17 | Ge Betz, Inc. | Methods and compositions for inhibiting polymerization of vinyl monomers |
| US6689926B2 (en) | 2002-02-12 | 2004-02-10 | Fina Technology, Inc. | Process for purifying styrene monomer feedstock prior to polymerization |
| CN107074990B (en) | 2014-10-14 | 2019-08-23 | 艺康美国股份有限公司 | Reduce polymer fouling and agglomeration in acrylate/salt/methacrylate/salt processes |
| CA2979828C (en) | 2015-03-18 | 2023-08-29 | Ecolab Usa Inc. | The use of stable lipophilic hydroxylamine compounds for inhibiting polymerization of vinyl monomers |
| US9957209B2 (en) | 2015-03-31 | 2018-05-01 | Ecolab Usa Inc. | Use of quinone methides as antipolymerants for vinylic monomers |
| US10155705B2 (en) * | 2015-04-20 | 2018-12-18 | Ecolab Usa Inc. | Sterically hindered hydroquinones as antifoulants for unsaturated monomers |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2329251A (en) * | 1941-01-21 | 1943-09-14 | Universal Oil Prod Co | Treatment of gasoline |
| US4011057A (en) * | 1974-04-16 | 1977-03-08 | E. I. Du Pont De Nemours And Company | Hindered phenol antioxidant composition containing an amino compound |
| US4296020A (en) * | 1979-10-29 | 1981-10-20 | Ici Americas Inc. | Polyurea thickened molding compositions |
| US4375006A (en) * | 1980-03-13 | 1983-02-22 | Ethyl Corporation | Stabilization of dibromostyrene |
| US4456526A (en) * | 1982-09-24 | 1984-06-26 | Atlantic Richfield Company | Method for minimizing fouling of heat exchangers |
| US4468343A (en) * | 1983-04-11 | 1984-08-28 | Cosden Technology, Inc. | Polymerization co-inhibitors for vinyl aromatic compounds |
| SE449561B (en) * | 1984-03-07 | 1987-05-11 | Regionala Stiftelsen I Vermlan | DEVICE INCLUDING A BEDDING LAYER PROVIDED TO BE PLACED UNDER A MATTRESS OR EQUIPMENT |
| US4744881A (en) * | 1984-12-05 | 1988-05-17 | Betz Laboratories, Inc. | Antioxidant material and its use |
| EP0230597B1 (en) * | 1985-12-19 | 1992-04-08 | Nippon Shokubai Kagaku Kogyo Co., Ltd | Method for inhibiting polymerization of maleimides |
| US4804956A (en) * | 1986-03-31 | 1989-02-14 | General Signal Corporation | Rearrangeable digital signal space division switching system |
| US4810354A (en) * | 1986-10-31 | 1989-03-07 | Betz Laboratories, Inc. | Bifunctional antifoulant compositions and methods |
| US4927561A (en) * | 1986-12-18 | 1990-05-22 | Betz Laboratories, Inc. | Multifunctional antifoulant compositions |
| US4867754A (en) * | 1988-05-24 | 1989-09-19 | Betz Laboratories, Inc. | Process and composition for stabilized distillate fuel oils |
| US5068271A (en) * | 1988-09-21 | 1991-11-26 | Uniroyal Chemical Company, Inc. | Arylenediamine substituted pyrimidines compositions |
| US4912247A (en) * | 1989-01-19 | 1990-03-27 | Betz Laboratories, Ltd. | Enhancement of aromatic amine inhibition of acrylate monomer polymerization by addition of mannich products |
| US5023372A (en) * | 1989-05-16 | 1991-06-11 | Betz Laboratories, Inc. | Methods and compositions for inhibiting (meth)acrylic acid polymerization |
| US4929778A (en) * | 1989-06-05 | 1990-05-29 | Betz Laboratories, Inc. | Methods and compositions for inhibiting styrene polymerization |
| US5039391A (en) * | 1991-01-03 | 1991-08-13 | Betz Laboratories, Inc. | Use of boron containing compounds and dihydroxybenzenes to reduce coking in coker furnaces |
-
1991
- 1991-07-22 US US07/733,480 patent/US5221498A/en not_active Expired - Fee Related
-
1992
- 1992-03-18 CA CA002063293A patent/CA2063293A1/en not_active Abandoned
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| US5221498A (en) | 1993-06-22 |
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